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Human Genome Region REGION135

Assembly:
GRCh38.p14
Location:
chr5:502,435-626,896
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KI270793.1 NT_187550.1 ALT Unavailable Unavailable Unavailable
           

REGION135 -- chr5 (CM000667.2):502,435-626,896